The Vancomycin−Nisin(1−12) Hybrid Restores Activity against Vancomycin Resistant Enterococci-Reference-Cited by-同舟云学术

The Vancomycin−Nisin(1−12) Hybrid Restores Activity against Vancomycin Resistant Enterococci

Published:2008-11-07 Issue:48 Volume:47 Page:12661-12663
ISSN:0006-2960
Container-title:Biochemistry
language:en
Short-container-title:Biochemistry

Author:

Arnusch Christopher J.¹,Bonvin Alexandre M. J. J.¹,Verel Anne Marie¹,Jansen Wouter T. M.¹,Liskamp Rob M. J.¹,de Kruijff Ben¹,Pieters Roland J.¹,Breukink Eefjan¹

Affiliation:

1. Department of Chemical Biology and Organic Chemistry, Institute of Biomembranes, and Department of NMR Spectroscopy, Bijvoet Center for Biomolecular Research, Science Faculty, Utrecht University, Padualaan 8, 3584 CH Utrecht, The Netherlands, Department of Medicinal Chemistry and Chemical Biology, Utrecht Institute for Pharmaceutical Sciences, Utrecht University, P.O. Box 80082, 3508 TB Utrecht, The Netherlands, and Department of Medical Microbiology, University Medical Center Utrecht, Heidelberglaan 100...

Publisher

American Chemical Society (ACS)

Subject

Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/bi801597b

Reference25 articles.

1. Use of the Cell Wall Precursor Lipid II by a Pore-Forming Peptide Antibiotic

2. Lipid II as a target for antibiotics

3. THE STRUCTURE AND MODE OF ACTION OF GLYCOPEPTIDE ANTIBIOTICS OF THE VANCOMYCIN GROUP

4. The nisin–lipid II complex reveals a pyrophosphate cage that provides a blueprint for novel antibiotics

5. Genetics and mechanisms of glycopeptide resistance in enterococci

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